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  • Latest
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    • News
      • "Being diagnosed with MS has changed my outlook in lots of ways"
      • "Cycling on closed roads with fellow enthusiasts is amazing!"
      • "I am not defined by having multiple sclerosis"
      • "I can’t remember what a healthy body feels like, but that’s ok, because I love my body and all it can still do"
      • "I might have MS but MS doesn't have me"
      • "It's OK if it's a shock to you" - people share their experiences of diagnosis with MS
      • "Live life to the fullest and accept any challenge that makes you look twice"
      • "MS doesn't stop me, it just makes me do things a little differently"
      • "Starting a podcast in lockdown helped us take ownership of the situation"
      • "Where you lose something, it makes you appreciate what you have"
      • "Writing poetry helped me come to terms with my MS diagnosis"
      • 'Coming out' about my MS
      • 'It used to be diagnose and adios, but now there is so much we can do'
      • 15 minutes with MS Trust Director of Information and Engagement Linden Muirhead
      • 15 minutes with MS Trust supporter Pia Reynolds
      • 15 minutes with MS blogger Amelia Southard
      • 15 minutes with MS nurse Verity Duff
      • 15 minutes with paediatric neurologist, Dr Evangeline Wassmer
      • 15 minutes with volunteer Will Berard
      • 15 minutes with... Friend of the MS Trust, Sam Bromfield
      • A buyer's guide to the Secret Art Show
      • A different perspective
      • A different perspective: my skydive
      • A magical experience
      • A personal interest in psychological support
      • A refreshing way to buy art
      • A sticky situation
      • A whole new world for me
      • Administering disease modifying drugs
      • Al and Bee's Mission:100
      • Amy's story
      • An MS diagnosis inspired me to set up my own business
      • An update on staffing at the MS Trust
      • Anti-LINGO-1, biotin and phenytoin results reported at AAN 2015
      • Artist's award winning design for the MS Trust
      • Ask the expert: Cognitive problems
      • Ask the expert: Coping with MS fatigue
      • Ask the expert: Disease modifying drugs
      • Ask the expert: Dizziness and balance
      • Ask the expert: MS pharmacists
      • Ask the expert: MS relapses
      • Ask the expert: Sex and MS
      • Ask the expert: heat sensitivity
      • Ask the expert: palliative care
      • Ask the expert: pregnancy and MS
      • Ask the expert: speech problems
      • Ask the expert: stem cell transplantation
      • Ask the expert: swallowing problems
      • Assisted dying
      • Assisted dying. Some thoughts, by Ian Daly
      • BBC Radio 1's Beccy Huxtable shares how the MS Trust supported her after diagnosis
      • BMA award honours for MS Trust resources
      • Back to school? Guidance for young people with MS
      • Being diagnosed with MS during lockdown
      • Bladder or bowel problems? You're not alone
      • Cabbages and an MS King
      • Call for national neurology plan following largest ever survey of people with neurological conditions
      • Can't take the heat?
      • Can’t change what happens, just have to deal with it - Wayne's Story
      • Celebrating 25 years of MS specialist nursing
      • Chair of Trustees, Caitlin and her husband Tim, talk about how the MS Trust helped them
      • Challenged myself to walk 150 miles throughout May
      • Chemical solvents, smoking and MS risk
      • Chilled out: cold sensitivity and MS
      • Choosing a disease modifying drug: Jo's story
      • Choosing my disease modifying drug
      • Christmas cards are here!
      • Clemastine may promote remyelination of optic nerve
      • Cocoa improves MS fatigue
      • Coffee Break: Five minutes with MS specialist nurse Michelle Meehan
      • Coming out of lockdown - slowly. But what do the new rules mean for people with MS?
      • Conference Raffle Test Page
      • Continuing to support health professionals as far as we can
      • Coronavirus COVID-19 and multiple sclerosis - update 13 March
      • Coronavirus COVID-19: what does it mean for people with multiple sclerosis?
      • Could stem cell therapy work for progressive MS?
      • Could you be an MSTV reporter?
      • Covid boosters and shielding changes for people with MS
      • Covid-19 treatments for people with MS
      • Covid-19 vaccine and MS: Your questions answered
      • Covid-19 vaccines and MS: Part two
      • Covid-19 vaccines and people with MS: side effects and the second dose
      • Covid-19 vaccines: what they mean for people with MS
      • Cycling 1,000km for the MS Trust
      • Cycling for my sister
      • DVLA medical questionnaire consultation
      • David's Diary - An afternoon volunteering with Cards for Good Causes
      • David's Diary: Inclusion and Diversity
      • David's diary - The challenges facing people with secondary progressive MS
      • Declutter and donate: Charlotte's story
      • Designing a robot to help people with MS
      • Diary of a relapse by Carla King
      • Diary of a steroid taker by Carla King
      • Disappointing topline results from high dose biotin study
      • Do you know what really gets on my nerves?
      • Drinking coffee may reduce the risk of developing multiple sclerosis
      • Drug for primary progressive MS licensed in the USA
      • EMA warns that Gilenya must not be taken during pregnancy
      • Enabled by design
      • Encouraging results from ozanimod drug trial
      • End of life planning: starting difficult conversations
      • European drug regulator recommends restricted use of Lemtrada
      • Explore London with 20in20 guided tours
      • Fampyra approved for use on the NHS in Scotland
      • Fampyra approved for use on the NHS in Wales
      • Five top tips for improving your lung health
      • Flu season 2020
      • Flu season 2021
      • Focus on: fact or fiction?
      • Focus on: self-compassion and resilience
      • Focus on: sleep problems in MS
      • Focus on: using orthoses to improve walking difficulties
      • Food and Fatigue
      • Food for thought
      • Gabapentin and pregabalin - new rules for prescriptions
      • Gemma's story - "All I remember him saying were the words ‘MS in your brain’ "
      • Gene discovered that can increase risk of rare form of progressive MS
      • Getting the early treatment debate into perspective
      • Getting to know my MS
      • Going boldly through the blue
      • Good news! NICE approves Ocrevus (ocrelizumab) for primary progressive multiple sclerosis
      • Grit and determination
      • Having a baby
      • Healthy hobbies
      • Heath Technology Wales guidance for AHSCT
      • Here we are again!
      • High dose biotin withdrawn from European licensing
      • How I coped being pregnant and diagnosed with MS during lockdown
      • How can we design services that work better for people with advanced MS?
      • How can we make MS care fair for people with progressive MS?
      • How could Brexit affect you, if you have MS?
      • How fundraising for the MS Trust helps me to help my daughter
      • How people react to my MS - Ian's story
      • How the MS Trust is helping people with MS make services more accessible, responsive and supportive
      • How to get the most out of virtual appointments
      • How to have yourself a merry little Christmas
      • How to stay calm and carry on during the coronavirus crisis when you have MS
      • How wheelchair basketball has helped with my MS
      • I adore 'the Proclaimers' and 500 miles was a fitting tribute to them
      • I am not lazy, merely fatigued - Will's story
      • I have MS therefore I am: on MS, philosophy and finding hope
      • I have MS. What should I do now?
      • I made my husband a hydration station during lockdown
      • I would like to say how proud I am of all of them
      • If we could raise money to help other people in need of support for the sake of a few blisters, then we will!
      • If you are thinking of supporting the MS Trust in these difficult times, we would encourage you to do it!
      • Information you can Trust
      • Introducing MS Decisions
      • Introducing Staying Smart
      • Introducing our new Advanced MS Champion for Cumbria
      • Introducing our new Advanced MS Champion for Swansea
      • Introducing the Heart of MS Care campaign
      • Introducing the lay members of MS Forward View
      • Is MS hereditary or not?
      • Is stem cell therapy right for my MS?
      • Jenna's treatment story: Mavenclad
      • Jim to trek from Land's End to John O'Groats
      • Juggling MS and family life: Five top tips
      • Julie Stevens
      • Katie's story: "My mum was diagnosed with MS when I was 14"
      • Kenny's remarkable journey
      • Kesimpta (ofatumumab) approved for relapsing remitting MS in Scotland
      • Lara’s story: “You can emerge in a new way”
      • Laura's story: my Covid-19 vaccine experience
      • Letisha's story
      • Letisha's story: Work and MS
      • Let’s make MS care fair!
      • Life changing: the hopes and fears of the MS community in 2022
      • Lis' MS journey: one woman and her bike
      • Living with MS and life at the Tower of London
      • Living with primary progressive MS: Yvonne's story
      • MS Decisions: Getting involved
      • MS Trust Home Festival name change
      • MS Trust fills the summer festival void with new fundraising event
      • MS Trust funded nurses in Lanarkshire have improved support and care for people with MS
      • MS Trust launches MS Decisions to support people making treatment decisions
      • MS Trust launches new campaign to support MS healthcare services
      • MS Trust leads new consensus on priorities to ensure a fair future for MS care
      • MS Trust report finds people with progressive MS feel like they're getting a second class service
      • MS Trust report shows that emergency admissions for people with MS continue to rise
      • MS Trust welcomes Panorama stem cell report, announces plans to audit stem cell services
      • MS and EBV in the news
      • MS and exercise - a Q&A with Henriette
      • MS and exercise: part four - a Q&A with physiotherapist, Henriette
      • MS and exercise: part three - a Q&A with physiotherapist, Henriette
      • MS and exercise: part two - a Q&A with physiotherapist, Henriette
      • MS and the menopause
      • MS in the Media - 1 June 2018
      • MS in the Media - 1 May 2020
      • MS in the Media - 1 November 2019
      • MS in the Media - 10 January 2020
      • MS in the Media - 10 May 2019
      • MS in the Media - 11 October 2019
      • MS in the Media - 12 April 2019
      • MS in the Media - 12 July 2019
      • MS in the Media - 13 December 2019
      • MS in the Media - 13 July
      • MS in the Media - 14 February 2020
      • MS in the Media - 15 January 2021
      • MS in the Media - 15 June 2018
      • MS in the Media - 15 March 2019
      • MS in the Media - 15 November 2019
      • MS in the Media - 16 August 2019
      • MS in the Media - 16 October 2020
      • MS in the Media - 17 April 2020
      • MS in the Media - 17 January 2020
      • MS in the Media - 17 May 2019
      • MS in the Media - 18 December 2020
      • MS in the Media - 18 September 2020
      • MS in the Media - 19 July 2019
      • MS in the Media - 19 June 2020
      • MS in the Media - 2 August 2019
      • MS in the Media - 2 October 2020
      • MS in the Media - 20 December 2019
      • MS in the Media - 20 July 2018
      • MS in the Media - 20 November 2020
      • MS in the Media - 21 August 2020
      • MS in the Media - 21 June 2019
      • MS in the Media - 22 June 2018
      • MS in the Media - 22 May 2020
      • MS in the Media - 22 November 2019
      • MS in the Media - 23 August 2019
      • MS in the Media - 24 April 2020
      • MS in the Media - 24 January 2020
      • MS in the Media - 24 May 2019
      • MS in the Media - 25 September 2020
      • MS in the Media - 26 July 2019
      • MS in the Media - 27 November 2020
      • MS in the Media - 27 September 2019
      • MS in the Media - 28 August 2020
      • MS in the Media - 28 February 2020
      • MS in the Media - 29 January 2021
      • MS in the Media - 29 November 2019
      • MS in the Media - 3 April 2020
      • MS in the Media - 3 May 2019
      • MS in the Media - 30 August 2019
      • MS in the Media - 31 May 2019
      • MS in the Media - 4 October 2019
      • MS in the Media - 4 September 2020
      • MS in the Media - 5 April 2019
      • MS in the Media - 5 July 2019
      • MS in the Media - 6 December 2019
      • MS in the Media - 6 July 2018
      • MS in the Media - 6 November 2020
      • MS in the Media - 6 September 2019
      • MS in the Media - 7 August 2020
      • MS in the Media - 7 February 2020
      • MS in the Media - 7 June 2019
      • MS in the Media - 8 November 2019
      • MS in the Media - 9 August 2019
      • MS in the Media - 9 October 2020
      • MS in the Media - ECTRIMS 2019
      • MS nurse takes on 2020 London Marathon
      • MS nurses – the good, the busy and the gaps in services
      • MS was my wake-up call to start living life to the full
      • Making our voices heard
      • Martin Baum on MS awareness week 2021
      • Me, Myself and MS
      • Mental health and MS: It's good to talk
      • Mission:100 Orkney vs Shetland
      • Multiple sclerosis and disease modifying drugs, what are my options?
      • My MS diagnosis story
      • My MS diagnosis story: "I was overwhelmed with the mix of emotions I was going through"
      • My MS diagnosis story: "It took me a long time to realise that it was okay not to be okay"
      • My MS to Asics 10km Story
      • My Vespa adventure for the MS Trust
      • My fundraising challenge to support my son and daughter-in-law
      • My journey to Russia for HSCT
      • My personal journey with HSCT
      • My search for MS support while studying for a PhD
      • NICE recruiting people living with MS and health professionals to update the MS Clinical Guideline
      • NICE rejects Sativex in draft guidance on cannabis-based medicinal products
      • Neurologists move toward earlier treatment for MS
      • Neuropathic pain - the 'invisible illness'
      • New guidelines for pregnancy in multiple sclerosis
      • New report calls for neurology care to be delivered closer to home
      • No link between vaccination and risk of MS
      • Ocrevus (ocrelizumab) for primary progressive MS – NICE confirms approval in final guidance
      • Ocrevus approved for primary progressive MS in Scotland
      • Ocrevus: What you need to know
      • Ofatumumab (Kesimpta) approved for relapsing MS in England and Wales
      • Ofatumumab (Kesimpta) gets UK licence for relapsing remitting MS
      • On the box: Hollyoaks set to tackle MS storyline
      • On ‘Coming Out’
      • One Cat and her dog
      • Overall health matters in MS
      • Ozanimod (Zeposia) - NICE says no in final decision
      • Ozanimod (Zeposia) approved for relapsing remitting MS in Scotland
      • Ozanimod (Zeposia) for relapsing remitting multiple sclerosis rejected by NICE
      • Ozanimod (Zeposia) recommended for European licence
      • PANORAMIC trial for Covid-19 treatment
      • Pass on something wonderful
      • Phoebe talks to us about being diagnosed with MS during lockdown.
      • Plegridy approved for relapsing remitting MS in England
      • Poetry and MS
      • Ponesimod (Ponvory) for relapsing remitting multiple sclerosis rejected by NICE
      • Ponvory (ponesimod) approved for relapsing remitting MS in Scotland
      • Preliminary research on Covid-19 in people with MS in Italy offers some reassurance
      • Providing the best service we can for people affected by MS
      • Putting MS specialists at the heart of MS care
      • Q&A with MS nurse Nicki Abel: Disease modifying drugs
      • Questions about shielding from 1st June
      • Receiving an MS diagnosis in lockdown ended my RAF dream
      • Reflections on the Great North Run
      • Regan's treatment story: Lemtrada
      • Remembering my sister with a 50-day cycle ride
      • Remyelination research: what it means for people with MS
      • Representing people with MS in the UK
      • Researchers develop mRNA vaccine to treat MS-like condition in mice
      • Reset and reform
      • Restarting our specialist nurse and advanced MS champion programmes
      • Sativex cost-effective in final NICE guideline on cannabis-based medicines
      • Sew-cially distancing fundraising ideas!
      • Should I be preparing now in case I catch coronavirus?
      • Should I be wearing a face covering during the COVID-19 outbreak?
      • Sign up to Miles for MS for FREE
      • Siponimod (Mayzent) approved for active secondary progressive MS in England and Wales
      • Siponimod (Mayzent) approved for active secondary progressive MS in Scotland
      • Siponimod for active secondary progressive MS rejected by Nice
      • Siponimod for secondary progressive MS: help us make the case to NICE
      • Siponimod granted European licence for active secondary progressive MS
      • Siponimod recommended for secondary progressive MS by European Medicines Agency
      • Staying connected
      • Sticks and stone may break my bones and your words DO hurt me
      • Stomach bacteria might protect against MS
      • Streaming for the win
      • Study finds poor integration between neurology and palliative care teams
      • Study shows Lemtrada improves disability in relapsing remitting MS
      • Support the MS Trust this April through Discount Promo Codes
      • Susan's story - My nurse gave me hope that I can actually have a life
      • Swallowing hard: dysphagia and MS
      • Taking a leap
      • Taking on Miles for MS for the MS Trust
      • Taking part in MS: Play was great fun!
      • Talking to your kids about MS
      • Temporary restriction on use of Lemtrada
      • Tesco stores in South West to collect funds for MS
      • Thank you for joining our campaign and raising awareness of MS!
      • Thanks to MS, I am learning to ride!
      • The MS Trust's Janice answers some of your coronavirus questions
      • The Walkie Talkies team conquer 100km of the Jurassic Coast for the MS Trust
      • The challenges of choosing a DMD as a new mother
      • The group of MS nurses covering 1,000 miles to say thank you for their education
      • The need for ‘MS Trust in us’ is so compelling
      • Top tips to help you stay connected during the COVID-19 crisis
      • Trial reports myelin repair success
      • Twelve year old Lacey hasn't been able to hug her dad for a year
      • UK’s top MS nurses, therapists and neurologists recognised in QuDoS awards shortlists
      • Under-the-skin injection of Tysabri gets licence in UK and Ireland
      • Unite Students
      • Update on coronavirus COVID-19 and multiple sclerosis
      • Update on the MS Trust's emergency appeal
      • Using creativity to cope with long-term conditions like MS
      • Walking difficulties: getting your walking back on track after lockdown
      • Walking in memory of my mum
      • Ways to manage pain for a comfortable winter
      • We are planning to make it an annual event!
      • What does the future look like for community MS support?
      • What it's like to be an Orthodox rabbi with SPMS during Hanukkah
      • What led Trishna to become a health and disability advocate?
      • What’s going on with Covid-19 medicines for people with MS?
      • When will people with MS get a covid vaccine?
      • Who gets MS and why?
      • Why I abseiled 400ft for the MS Trust
      • Why I wanted to become a Friend of the MS Trust
      • Why I’m releasing a charity Christmas song for the MS Trust
      • Work and MS: Five top tips
      • Would having children be impossibly hard for me, my partner, and the children themselves?
      • “I didn’t receive any information about MS when I was diagnosed. Nothing.” – Leonie’s story
      • “My mummy’s got wheels!”: managing MS while bringing up my four-year-old son
      • “When I met my MS nurse everything started to make sense”
    • Research
      • Brain training: a cognitive rehabilitation programme evaluated
      • Can exercise therapy started soon after diagnosis affect the course of multiple sclerosis?
      • Can standing frames improve mobility in progressive MS?
      • Coronavirus COVID-19 and multiple sclerosis
      • Daytime sleepiness and driving in MS
      • Do disease modifying drugs affect life expectancy?
      • Do medicines reduce fatigue in MS?
      • Effect of vitamin D supplements on MS activity
      • Exercise is good for your brain
      • Fampyra rejected in draft update to NICE MS Clinical Guideline
      • Finding your way; how does MS affect navigation skills?
      • How do families affected by MS manage health information?
      • How does multiple sclerosis affect dating and romantic relationships?
      • How long does it take for an MS drug to be fully effective?
      • How quickly do people with MS recover from Covid-19?
      • Is a ketogenic diet good for people with multiple sclerosis?
      • Learning a second language improves brain structures in MS
      • MRI reveals smouldering MS lesions
      • MS onset in childhood: do disease modifying drugs delay long term disability?
      • MS research update - Exercise early in the course of MS and FES effects on bladder symptoms - 31 July 2018
      • MS research update - The right word won't come to me... A study looking at slowed word retrieval in MS - 21 October 2013
      • MS research update – Abdominal massage for constipation – 4 December 2018
      • MS research update – Cell therapy targeting Epstein-Barr virus tested in progressive MS – 20 December 2018
      • MS research update – Could cocoa help MS fatigue? – 15 October 2018
      • MS research update – Factors affecting DMD prescribing in the UK – 21 January 2019
      • MS research update – Walking improves with mental rehearsal – 8 November 2018
      • Machine learning identifies new subtypes of MS from MRI scans
      • Mayzent (siponimod) use expanded in England for secondary progressive multiple sclerosis
      • Microaggressions at work; more than just hurt feelings
      • New report highlights barriers to accessing Sativex across the UK
      • New study provides strong evidence for role of Epstein Barr virus as a trigger multiple sclerosis
      • Ponvory (ponesimod) approved for relapsing remitting MS in England and Wales
      • Remyelination – what progress has been made?
      • Stem cell transplants in the news
      • Temelimab: early clinical trial suggests potential for remyelination
      • Testing iStep-MS, a new programme to encourage physical activity
      • Treatments for foot drop compared
      • Tysabri risk of PML with extended interval dosing
      • Vumerity (diroximel fumarate) approved for relapsing remitting MS in England and Wales
      • Vumerity (diroximel fumarate) approved for relapsing remitting MS in Scotland

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Multiple Sclerosis Trust

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